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临床监查员CRA I

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Onsite

临床监查员CRA I

上海康德弘翼医学临床研究有限公司

临床监查员CRA I

Skills

Google Cloud PlatformCompliance

1 year ago

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Important information


Contract type:

Permanent

Location:

Fuzhou, Fujian, China

Work mode:

Onsite

Published on:

13 August 2026

What they need


该职位来源于猎聘 职责描述:

  • Implements and monitors local clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH‐GCP guidelines
  • Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites
  • Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely
  • Provides regular site status information to team members, trial management, and updates trial management tool.
  • Completes monitoring activity documents as required by Company or Sponsor SOPs or other contractual obligations
  • Works closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues
  • Escalates site and trial related issues per Company SOPs, until identified issues are resolved or closed
  • Performs essential document site file reconciliation
  • Performs source document verification and query resolution
  • Assesses IP accountability, dispensation, and compliance at the investigative sites
  • Verifies Serious Adverse Event (SAE) reporting according to trial specifications and relevant local and ICH GCP guidelines
  • Communicates with investigative sites
  • Updates applicable tracking systems
  • Ensures all required training is completed and documented
  • Be assigned logistical support tasks by CTM for Investigator Meetings 任职要求:
  • Education

Undergraduate degree or its international equivalent in clinical, science, or health‐related field from an accredited institution; a licensed health‐care professional (i.e., registered nurse); or equivalent work experience required

  • Experience

1to 2 years of local trial experience; exposure to MNC and global trials

  • Preferred Education and/or Experience

Clinical research experience

Knowledge of ICH and local regulatory authority regulations regarding drug

An advanced degree (e.g., M.S.,M.B.A., PharmD, etc.)

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